Sharifia Wills

Regulatory Scientist - Chemistry, Manufacturing and Controls @Cardinal Health

San Francisco, CA, US
EMAILS
s••••••••@cardinalhealth.com
MOBILE NUMBERS
+15•••••••06

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WORK HISTORY

Nov 2021 — Present

Regulatory Scientist - Chemistry, Manufacturing and Controls @Cardinal Health

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San Francisco, CA, US

Knowledge of global CMC regulations and guidelines -Provide technical support and research for CMC change management -Assist with global regulatory assessments and implementation of regulatory strategy for product dossiers-Prepare, author, and maintain global regulatory dossiers -Proficient in Common Technical Document (CTD) format and content -Contemporization of traditional formatted documents into the CTD -Meeting company and client milestones with a focus on quality and timely submissions -Cross functional collaboration with stakeholders and supports multiple projects -Proficient in client network systems

EDUCATION

2008 — 2013

The Johns Hopkins University

Postdoctoral Fellowship, The Johns Hopkins School of Medicine, Neuroimmunopathology Laboratory

1995 — 1999

Xavier University of Louisiana

BS, Biology

1999 — 1999

Center for Cross-Cultural Study, Seville Spain

Intensive Language Training Program

2002 — 2008

University of California, Davis

PhD, Immunology

2013 — 2014

Keck Graduate Institute

Postdoctoral Professional Masters, Bioscience Management

SKILLS

Cell BiologyBiotechnologyTeamworkTissue CultureConfocal MicroscopyProtocolGmpMolecular BiologyFluorescence MicroscopyCorrective and Preventive Action (Capa)Market AnalysisCell CultureProject ManagementImmunohistochemistryPolymerase Chain Reaction (Pcr)ImmunofluorescenceU.s. Food and Drug Administration (Fda)Market ResearchElisaStandard Operating Procedure (Sop)CellLife SciencesCross-Functional Team LeadershipCompetitive IntelligenceMarketing StrategyImmunologyKepner-TregoeFlow CytometryRegulatory AffairsLifesciencesBusiness StrategyMedical DevicesLaboratory SkillsPcrIn VitroProblem SolvingNeuroscienceWestern Blotting

ABOUT SHARIFIA WILLS

Neuroimmunologist with training in MBA-level management and advanced business practices in the life sciences industry. My interest lies in the intersection of scientific knowledge and the path of drugs and medical devices moving safely and effectively from the bench to the bedside for patients. The focus of my Postdoctoral Professional Masters education was regulatory affairs. Regulatory Affairs Certification (RAC-Global).

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